Cas 294637-23-3,4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

294637-23-3

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Basic information

Product Name: 4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
Synonyms: 4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
CAS NO:294637-23-3
Molecular Formula:
Molecular Weight: 388.38
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(294637-23-3)
EPA Substance Registry System: 4-(R)-azido-3a-hydroxy-6-oxo-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester(294637-23-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 294637-23-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 294637-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,6,3 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 294637-23:
(8*2)+(7*9)+(6*4)+(5*6)+(4*3)+(3*7)+(2*2)+(1*3)=173
173 % 10 = 3
So 294637-23-3 is a valid CAS Registry Number.

294637-23-3Upstream product

144534-49-6 (2S,3aR,7aR)-3a-hydroxy-6-oxo-2,3,3a,6,7,7a-hexahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

294637-23-3Downstream Products

294637-26-6 (2S,3aS,4R,6R,7aR)-4-Azido-6-(tert-butyl-dimethyl-silanyloxy)-3a-hydroxy-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

294637-23-3Relevant academic research and scientific papers

Radical cleavage of a β-hydroxy azide: A reversal of regioselectivity in the oxidative fragmentation of hydroindoles

Wipf, Peter,Mareska, David A.

, p. 4723 - 4727 (2000)

Treatment of hydroindole 17 with PhI(OAc)2/I2 leads to oxidative fragmentation of the β-hydroxy azide moiety and results in the exclusive formation of keto nitrile 18 via radical cleavage of the lateral ring C-C bond. (C) 2000 Elsevier Science Ltd.

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